JP6431095B2 - Chia seed derived composition - Google Patents
Chia seed derived composition Download PDFInfo
- Publication number
- JP6431095B2 JP6431095B2 JP2016569324A JP2016569324A JP6431095B2 JP 6431095 B2 JP6431095 B2 JP 6431095B2 JP 2016569324 A JP2016569324 A JP 2016569324A JP 2016569324 A JP2016569324 A JP 2016569324A JP 6431095 B2 JP6431095 B2 JP 6431095B2
- Authority
- JP
- Japan
- Prior art keywords
- composition
- chia
- water
- seed
- polysaccharide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000000203 mixture Substances 0.000 title claims description 102
- 235000020235 chia seed Nutrition 0.000 title claims description 54
- 229920001282 polysaccharide Polymers 0.000 claims description 61
- 239000005017 polysaccharide Substances 0.000 claims description 61
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 48
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- 108090000623 proteins and genes Proteins 0.000 claims description 11
- 102000004169 proteins and genes Human genes 0.000 claims description 11
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- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 239000008107 starch Substances 0.000 claims description 6
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- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
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- 238000004904 shortening Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- KZJWDPNRJALLNS-VJSFXXLFSA-N sitosterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CC[C@@H](CC)C(C)C)[C@@]1(C)CC2 KZJWDPNRJALLNS-VJSFXXLFSA-N 0.000 description 1
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- 229950005143 sitosterol Drugs 0.000 description 1
- NLQLSVXGSXCXFE-UHFFFAOYSA-N sitosterol Natural products CC=C(/CCC(C)C1CC2C3=CCC4C(C)C(O)CCC4(C)C3CCC2(C)C1)C(C)C NLQLSVXGSXCXFE-UHFFFAOYSA-N 0.000 description 1
- 235000020183 skimmed milk Nutrition 0.000 description 1
- 239000002884 skin cream Substances 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
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- 229940005581 sodium lactate Drugs 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
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- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- KJCLYACXIWMFCC-UHFFFAOYSA-M sodium;5-benzoyl-4-hydroxy-2-methoxybenzenesulfonate Chemical compound [Na+].C1=C(S([O-])(=O)=O)C(OC)=CC(O)=C1C(=O)C1=CC=CC=C1 KJCLYACXIWMFCC-UHFFFAOYSA-M 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
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- TUHBEKDERLKLEC-UHFFFAOYSA-N squalene Natural products CC(=CCCC(=CCCC(=CCCC=C(/C)CCC=C(/C)CC=C(C)C)C)C)C TUHBEKDERLKLEC-UHFFFAOYSA-N 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 150000003432 sterols Chemical class 0.000 description 1
- 235000003702 sterols Nutrition 0.000 description 1
- WPLOVIFNBMNBPD-ATHMIXSHSA-N subtilin Chemical compound CC1SCC(NC2=O)C(=O)NC(CC(N)=O)C(=O)NC(C(=O)NC(CCCCN)C(=O)NC(C(C)CC)C(=O)NC(=C)C(=O)NC(CCCCN)C(O)=O)CSC(C)C2NC(=O)C(CC(C)C)NC(=O)C1NC(=O)C(CCC(N)=O)NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C1NC(=O)C(=C/C)/NC(=O)C(CCC(N)=O)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)CNC(=O)C(NC(=O)C(NC(=O)C2NC(=O)CNC(=O)C3CCCN3C(=O)C(NC(=O)C3NC(=O)C(CC(C)C)NC(=O)C(=C)NC(=O)C(CCC(O)=O)NC(=O)C(NC(=O)C(CCCCN)NC(=O)C(N)CC=4C5=CC=CC=C5NC=4)CSC3)C(C)SC2)C(C)C)C(C)SC1)CC1=CC=CC=C1 WPLOVIFNBMNBPD-ATHMIXSHSA-N 0.000 description 1
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- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 229960005349 sulfur Drugs 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 230000009469 supplementation Effects 0.000 description 1
- 230000009747 swallowing Effects 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 210000001541 thymus gland Anatomy 0.000 description 1
- 239000001585 thymus vulgaris Substances 0.000 description 1
- LOIYMIARKYCTBW-OWOJBTEDSA-N trans-urocanic acid Chemical compound OC(=O)\C=C\C1=CNC=N1 LOIYMIARKYCTBW-OWOJBTEDSA-N 0.000 description 1
- LOIYMIARKYCTBW-UHFFFAOYSA-N trans-urocanic acid Natural products OC(=O)C=CC1=CNC=N1 LOIYMIARKYCTBW-UHFFFAOYSA-N 0.000 description 1
- ICUTUKXCWQYESQ-UHFFFAOYSA-N triclocarban Chemical compound C1=CC(Cl)=CC=C1NC(=O)NC1=CC=C(Cl)C(Cl)=C1 ICUTUKXCWQYESQ-UHFFFAOYSA-N 0.000 description 1
- 229960001325 triclocarban Drugs 0.000 description 1
- VLPFTAMPNXLGLX-UHFFFAOYSA-N trioctanoin Chemical compound CCCCCCCC(=O)OCC(OC(=O)CCCCCCC)COC(=O)CCCCCCC VLPFTAMPNXLGLX-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- MECHNRXZTMCUDQ-RKHKHRCZSA-N vitamin D2 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)/C=C/[C@H](C)C(C)C)=C\C=C1\C[C@@H](O)CCC1=C MECHNRXZTMCUDQ-RKHKHRCZSA-N 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 239000010497 wheat germ oil Substances 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 235000013618 yogurt Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
- 239000001243 zingiber officinale rosc. root absolute Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
- A61K8/9783—Angiosperms [Magnoliophyta]
- A61K8/9789—Magnoliopsida [dicotyledons]
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Preparation or treatment thereof
- A23L2/38—Other non-alcoholic beverages
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Preparation or treatment thereof
- A23L2/52—Adding ingredients
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/10—Natural spices, flavouring agents or condiments; Extracts thereof
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Polymers & Plastics (AREA)
- Food Science & Technology (AREA)
- Nutrition Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Mycology (AREA)
- Biotechnology (AREA)
- Botany (AREA)
- Microbiology (AREA)
- Dispersion Chemistry (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Non-Alcoholic Beverages (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Seasonings (AREA)
Description
本発明は、チアシード由来組成物に関する。 The present invention relates to a chia seed-derived composition.
チアシード(Chia Seed)は、シソ科サルビア属に属する植物の種子であり、直径が約2mmの黒ゴマ様のものである。チアシードは、メキシコ、アルゼンチン、ボリビアなどで多く栽培されており、南米では一般的に食物として用いられている。チアシードを水に浸すと、種子の周囲に透明な物質が膨らんでくる。膨張する割合は非常に大きく、約10倍程度にもなる。このため膨張後には、丁度カエルの卵のような様子となる。チアシードは多くの油脂を含んでおり、この油脂のみを採取して、チアシードオイルとしても用いられている。
チアシードには、脂肪の吸収阻害作用(特許文献1)や性機能の改善作用(特許文献2)があると言われており、研究が行われている。
一方、化粧料を用いる重要な目的の一つに皮膚の改善、すなわち、肌荒れ、カミソリ負け、日焼け後のほてり等の改善等が挙げられる。そして、現在、この目的のために多種の化粧料が提供されている。現在提供されているこれらの化粧料は、高度の皮膚改善効果を提供するために油分が配合されているのが常である。また、この油分が配合された化粧料の経時安定性を担保するために界面活性剤を配合するのも常である。そして、この界面活性剤の配合により、優れた乳化安定性を有する化粧料が得られる反面、べたついた使用感をも伴う傾向にある。Chia Seed is a seed of a plant belonging to the genus Salvia, and has a black sesame-like shape with a diameter of about 2 mm. Chia seeds are often cultivated in Mexico, Argentina, Bolivia, etc., and are generally used as food in South America. When a chia seed is immersed in water, a transparent substance swells around the seed. The rate of expansion is very large, about 10 times. For this reason, after expansion, it looks just like a frog egg. Chia seed contains a lot of fats and oils, and only these fats and oils are collected and used as chia seed oil.
Chia seeds are said to have fat absorption inhibitory action (Patent Document 1) and sexual function improving action (Patent Document 2), and are being studied.
On the other hand, one of the important purposes of using cosmetics is to improve skin, that is, to improve rough skin, razor loss, hot flash after sunburn, and the like. Currently, various cosmetics are provided for this purpose. These cosmetics currently provided usually contain oils to provide a high skin improvement effect. Moreover, it is usual to mix | blend surfactant in order to ensure the temporal stability of the cosmetics by which this oil component was mix | blended. And, by blending this surfactant, a cosmetic having excellent emulsification stability can be obtained, but it also tends to have a sticky feeling.
従来、チアシードオイルを抽出する場合には、水に浸したときに膨張してくる透明な物質は廃棄される。このため、オイルを抽出するための種子部分と、周囲の透明な物質とを分離できれば、資源の有効活用の点で好ましい。
植物からの多糖類を製造する方法として、強アルカリ(水酸化ナトリウム(NaOH)溶液等)や強酸(塩酸(HCl)溶液等)を用いて分解する方法があるが、ほとんどが単糖まで分解されてしまい、多糖類としての特長を失う。
また、チアシードの場合、多糖類は種子外殻に固着しており、種子を傷付けずに分離する方法は開発されていない。
チアシードの種子内部にはΩ3を豊富に含む脂質やたんぱく質が多く含まれているため、種子を傷つければ、種子内成分の分離・活用が困難になる。
また、種子成分が外殻多糖類に混入すると、異臭や色調に問題が生じ、食品や化粧品への応用にも制限が生じる。
本発明は、上記した事情に鑑みてなされたものであり、その目的は、チアシード由来の種子と、それ以外の組成物とを分離して提供することである。
また、第二の目的として、さっぱりした使用感を保ちつつ、優れた皮膚改善効果を有し、さらに従来から乳化剤として汎用されてきた界面活性剤を配合することなしに経時的安定性に優れた、化粧料として用いることのできる乳化組成物を提供することである。Conventionally, when extracting chia seed oil, the transparent substance that expands when immersed in water is discarded. For this reason, it is preferable in terms of effective utilization of resources if the seed part for extracting the oil and the surrounding transparent substance can be separated.
As a method for producing polysaccharides from plants, there is a method using a strong alkali (such as sodium hydroxide (NaOH) solution) or a strong acid (such as hydrochloric acid (HCl) solution), but most of them are decomposed to monosaccharides. It loses its characteristics as a polysaccharide.
In the case of chia seed, the polysaccharide is fixed to the seed shell, and a method for separating the seed without damaging the seed has not been developed.
The seeds of chia seeds contain a lot of lipids and proteins rich in Ω3, so if the seeds are damaged, it becomes difficult to separate and utilize the components in the seeds.
Moreover, when a seed component mixes with a shell polysaccharide, a problem will arise in a strange odor and a color tone, and the application to food and cosmetics will also be restrict | limited.
This invention is made | formed in view of an above-described situation, The objective is to isolate | separate and provide the seed derived from a chia seed, and a composition other than that.
In addition, as a second purpose, while maintaining a refreshing feeling of use, it has an excellent skin improvement effect, and also has excellent temporal stability without blending a surfactant that has been widely used as an emulsifier in the past. It is to provide an emulsified composition that can be used as a cosmetic.
上記目的を達成するための第一の発明に係る種子は、チアシードに対して5〜50倍量の水を加え、種子外周のチア外殻多糖類を膨潤させた後、物理的な力を加えて、前記チア外殻多糖類を取り去って得られたことを特徴とする。
また、第二の発明に係る組成物は、チアシードに対して5〜50倍量の水を加え、種子外周のチア外殻多糖類を膨潤させた後、物理的な力を加えて、前記種子を取り去って得られた種子以外のチア外殻多糖類を主成分とする液体組成物またはこの液体組成物を乾燥させた粉末状組成物であることを特徴とする。
上記発明において、物理的な力が、攪拌機を用いて処理した後に、遠心処理することが好ましい。また、攪拌機を用いた処理が、回転数500rpm〜10000rpm、攪拌羽と外壁とのクリアランスが1mm〜100mmの条件にて攪拌させることが好ましい。
また、物理的な力が、種子を通過させる一方、膨潤したチア外殻多糖類の通過を規制する孔縁を備えた孔部の通過によって与えられることが好ましい。
また、前記組成物中の脂質が0.1%〜5%であることが好ましい。また、前記組成物中のタンパク質が0.1%〜10%、灰分が0.1%〜10%であることが好ましい。
このとき、前記組成物を固形分が10%となるよう水に溶解分散させた際の粘度が10mPa・s〜10000mPa・sであることが好ましい。
また、前記組成物の透明度は、660nmの波長で測定したABS値が0.1%水溶液で0.008以下で透明、1%水溶液で0.200〜0.500であることが好ましい。
また、前記組成物1gに対して30gの水を含水させた際の保水量が1gあたり10g〜20gであることが好ましい。
また、前記組成物中の多糖類の分子量が、5000(5×103)〜10000000(1×107)であることが好ましい。In order to achieve the above object, the seed according to the first invention adds 5 to 50 times the amount of water to the chia seed, swells the chia shell polysaccharide around the seed, and then applies physical force. And obtained by removing the above-mentioned thia outer polysaccharide.
In addition, the composition according to the second aspect of the present invention includes adding 5 to 50 times the amount of water to the chia seed, swelling the chia shell polysaccharide around the seed, and then applying physical force to the seed. It is characterized by being a liquid composition containing chia shell polysaccharides other than seeds obtained as a main component, or a powdered composition obtained by drying this liquid composition.
In the said invention, it is preferable to centrifuge after physical force processes using a stirrer. Moreover, it is preferable to stir the treatment using a stirrer under the conditions that the rotational speed is 500 rpm to 10,000 rpm and the clearance between the stirring blade and the outer wall is 1 mm to 100 mm.
It is also preferred that the physical force is provided by the passage of the pores with pore edges that allow the seeds to pass while restricting the passage of the swollen thiacopolysaccharide.
Further, the lipid in the composition is preferably 0.1% to 5%. The protein in the composition is preferably 0.1% to 10% and the ash content is preferably 0.1% to 10%.
At this time, the viscosity when the composition is dissolved and dispersed in water so that the solid content is 10% is preferably 10 mPa · s to 10000 mPa · s.
Further, the transparency of the composition is preferably transparent when the ABS value measured at a wavelength of 660 nm is 0.008 or less for a 0.1% aqueous solution and 0.200 to 0.500 for a 1% aqueous solution.
Moreover, it is preferable that the water-holding amount when 30 g of water is contained per 1 g of the composition is 10 g to 20 g per 1 g.
The molecular weight of the polysaccharide in the composition is preferably 5000 (5 × 10 3 ) to 10000000 (1 × 10 7 ).
また、結晶化変化、タンパクの変性を抑えるために澱粉及び/またはタンパクを含む食品と併用されることが好ましい。
また、上記組成物は、食品、飲料、調味料に含有させることができる。
このとき、調味料としては、上記組成物を0.5〜2質量%含み、400mPa・s〜5000mPa・s(B型粘度計、12rpm)の粘性を付与することが好ましい。
また、上記組成物と、乳化剤、保湿剤、増粘剤、抗酸化剤、保形剤及び染色剤からなる群から選択される少なくとも一つを併用してなる化粧素材とすることができる。
また、飲料には、上記組成物を0.1〜2質量%含み、軽度の粘性を付与することが好ましい。水分補給とミネラルやビタミンの補給は、熱中症予防には不可欠である。一方、喉の渇きを潤すためにも水分を補給するが、(その際「水は噛んで飲め」と言われるように、)一度に多くの水分を摂ることは、体力を消耗させ、胃腸などの消化器官に不快感を与えることがある。適度な粘性を持つ飲料は、口腔内から食道を緩やかに流れ、喉の渇き感を軽減する。また、香りの高い飲料の場合には、その芳醇な香りを長く楽しむことにも寄与する。上記組成物はベトツキ感が少なく、すべりの良い多糖類であり、清涼飲料などにも適している。
また、上記組成物をシャーベット等の氷菓に対し、0.5〜5.0質量%添加することが好ましい。この構成によれば、凍結後の結晶水を小さくすることができ、口当たりが向上する。Further, it is preferably used in combination with food containing starch and / or protein in order to suppress crystallization change and protein denaturation.
Moreover, the said composition can be contained in a foodstuff, a drink, and a seasoning.
At this time, the seasoning preferably contains 0.5 to 2% by mass of the above composition and imparts a viscosity of 400 mPa · s to 5000 mPa · s (B-type viscometer, 12 rpm).
Moreover, it can be set as the cosmetic material which uses together the said composition and at least 1 selected from the group which consists of an emulsifier, a moisturizer, a thickener, an antioxidant, a shape retention agent, and a dyeing agent.
The beverage preferably contains 0.1 to 2% by mass of the above composition and imparts a mild viscosity. Hydration and mineral and vitamin supplementation are essential to prevent heat stroke. On the other hand, water is replenished to relieve thirst, but taking a lot of water at one time (as it is said that “water can be chewed and drunk”) consumes physical strength, May cause discomfort in the digestive system. Beverages with moderate viscosity flow gently through the esophagus from the mouth, reducing the feeling of thirst. In the case of a highly fragrant beverage, it also contributes to enjoying the rich fragrance for a long time. The above-mentioned composition is a polysaccharide with little stickiness and is suitable for soft drinks and the like.
Moreover, it is preferable to add the said composition 0.5-5.0 mass% with respect to ice confectionery, such as a sherbet. According to this configuration, the water of crystallization after freezing can be reduced, and the mouthfeel is improved.
また、上記組成物を食品に添加して、とろみ剤として用いることが好ましい。嚥下困難者や高齢者向け食品には、適度な強度のゲル状体を達成できるとろみ剤が望まれている。理想的なとろみ剤は、溶解時に容易に溶け、とろみが付く時間が短く、また溶け残り(ダマ)が起こりにくく物が良い。また、様々な食材に使用されるため、溶解後の透明性や異臭が無いこと、さらにとろみ剤自体に味がないことが望ましい。
上記組成物は、容易に溶け溶け残り(ダマ)も起こりにくい。また、高粘度で且つチキソトロピー性を有し、とろみ剤としてべたつき感が無く、また食材の滑りも良くなることから、スムーズに飲み込むことが可能となり、誤嚥のリスクを減らすことができる。
チアシードの種子内部にはΩ3を豊富に含む脂質やたんぱく質、ミネラル類が多く含まれている。本発明によれば、種子外殻表面の粘質性多糖類を除去することにより、これらの健康維持に寄与する栄養成分を効率よく抽出、分離し、広く食品、化粧品、医薬品に応用することが可能になる。Moreover, it is preferable to add the said composition to a foodstuff and to use as a thickening agent. For foods for those with difficulty in swallowing and elderly people, a thickening agent that can achieve a gel-like body with an appropriate strength is desired. An ideal thickening agent dissolves easily when dissolved, has a short time for thickening, and is less likely to remain undissolved (dama). Moreover, since it is used for various foodstuffs, it is desirable that there is no transparency and no strange odor after dissolution, and that the thickener itself has no taste.
The composition is easily melted and hardly remains undissolved (dama). Moreover, it has high viscosity and thixotropy, does not feel sticky as a thickening agent, and improves the slipping of the food, so that it can be swallowed smoothly and the risk of aspiration can be reduced.
Chia seeds are rich in lipids, proteins and minerals rich in Ω3. According to the present invention, by removing the viscous polysaccharides on the surface of the seed shell, it is possible to efficiently extract and isolate these nutritional components that contribute to health maintenance, and can be widely applied to foods, cosmetics, and pharmaceuticals. It becomes possible.
また、上記第二の目的を解決するために、チアシード由来組成物を配合することにより、さっぱりした使用感を保ちつつ、優れた皮膚改善効果を有し、さらに従来から乳化剤として汎用されてきた界面活性剤を配合することなしに経時安定性に優れた乳化組成物を提供し得ることを見出し、基本的には本発明を完成した。すなわち、本発明者は以下に示す乳化組成物を提供する。
上記発明において、チアシード由来組成物を含んでなる乳化組成物を提供する。
上記チアシード由来組成物は、乳化組成物全体に対して、0.0001質量%〜10質量%(好ましくは、0.01質量%〜5.5質量%)であることが好ましい。
またこのとき、実質的に界面活性剤を配合しないことが好ましい。
本発明のチアシード由来組成物の化粧品への配合量は、乳化組成物全体に対して、0.0001質量%〜20質量%であることが好ましく、0.01質量%〜5.5質量%であることが更に好ましい。
チアシード由来組成物が乳化組成物全体に対して、0.0001質量%未満の場合には、本発明の所期の効果を十分に発揮させることができず好ましくない。また、乳化物全体に対して20質量%を越えて配合した場合には、配合量の増大に見合った効果の増強が期待できないだけではなく、製剤上も好ましくない。
また、チアシード由来組成物が乳化組成物全体の0.01質量%未満では、本発明品を配合したことによる十分な効果を得ることができず、10質量%を越えると乳化組成物がべたついた使用感を伴うことになり好ましくない。In addition, in order to solve the second object, by blending a chia seed-derived composition, while maintaining a refreshing feeling of use, it has an excellent skin improvement effect, and has been conventionally used as an emulsifier. It was found that an emulsified composition having excellent stability over time could be provided without blending an activator, and the present invention was basically completed. That is, this inventor provides the emulsion composition shown below.
In the said invention, the emulsion composition which comprises a chia seed origin composition is provided.
It is preferable that the said chia seed origin composition is 0.0001 mass%-10 mass% (preferably 0.01 mass%-5.5 mass%) with respect to the whole emulsion composition.
At this time, it is preferable that substantially no surfactant is blended.
The blending amount of the chia seed-derived composition of the present invention into the cosmetic is preferably 0.0001% by mass to 20% by mass, and 0.01% by mass to 5.5% by mass with respect to the entire emulsion composition. More preferably it is.
When the chia seed-derived composition is less than 0.0001% by mass with respect to the whole emulsion composition, the desired effect of the present invention cannot be exhibited sufficiently, which is not preferable. Moreover, when it mix | blends exceeding 20 mass% with respect to the whole emulsion, not only the increase | augmentation of the effect corresponding to the increase in a compounding quantity cannot be expected, but it is unpreferable also on a formulation.
In addition, when the chia seed-derived composition is less than 0.01% by mass of the entire emulsion composition, sufficient effects cannot be obtained by blending the product of the present invention, and when it exceeds 10% by mass, the emulsion composition becomes sticky. It is not preferable because it involves a feeling of use.
驚くべきことに、本発明のチアシード由来組成物を所定の割合で配合することにより、さっぱりした使用感を保ちつつ、優れた皮膚改善効果を有し、さらに従来から乳化剤として汎用されてきた界面活性剤を配合することなしに経時安定性に優れる乳化組成物が提供される。
しかしながら、後述するように、上記界面活性剤の本発明品含有化粧品中への配合が妨げられるものではない。
なお、これらの所期の効果は、上記有効成分を本発明品含有化粧品中に配合することのみで十分発揮させることができる。すなわち、専ら上記の効果の発揮のために、他の有効成分を追加配合する必要は特にない。ただし、他の薬効成分の配合により、乳化組成物が一般的に奏するであろう効果を付与する目的で、この他の薬効成分を本発明品含有化粧品中に配合することは、その配合により本発明の所期の効果を損なわない範囲で可能である。Surprisingly, by blending the chia seed-derived composition of the present invention at a predetermined ratio, it has an excellent skin improvement effect while maintaining a refreshing feeling of use, and has been conventionally used as an emulsifier. An emulsified composition having excellent stability over time without blending an agent is provided.
However, as will be described later, the incorporation of the surfactant into the cosmetics containing the product of the present invention is not hindered.
In addition, these desired effects can be sufficiently exerted only by blending the above active ingredient into the cosmetics containing the product of the present invention. That is, it is not particularly necessary to add other active ingredients exclusively for exhibiting the above effects. However, the blending of other medicinal ingredients in the cosmetics containing the present invention for the purpose of imparting an effect that the emulsion composition will generally exhibit by the blending of other medicinal ingredients is based on the blending. This is possible as long as the desired effect of the invention is not impaired.
例えば、本発明品含有化粧品中をサンケア製品として用いる場合には、パラアミノ安息香酸等の安息香酸系紫外線吸収剤;アントラニル酸メチル等のアントラニル酸系紫外線吸収剤;サリチル酸オクチル、サリチル酸フェニル、サリチル酸ホモメンチル等のサリチル酸系紫外線吸収剤;パラメトキシケイ皮酸イソプロピル、パラメトキシケイ皮酸オクチル、パラメトキシケイ皮酸−2−エチルヘキシル、ジパラメトキシケイ皮酸モノ−2−エチルヘキサン酸グリセリル、〔4−ビス(トリメチルシロキシ)メチルシリル−3−メチルブチル〕−3、4、5−トリメトキシケイ皮酸エステル等のケイ皮酸系紫外線吸収剤;2、4−ジヒドロキシベンゾフェノン、2−ヒドロキシ−4−メトキシベンゾフェノン、2−ヒドロキシ−4−メトキシベンゾフェノン−5−スルホン酸、2−ヒドロキシ−4−メトキシベンゾフェノン−5−スルホン酸ナトリウム等のベンゾフェノン系紫外線吸収剤;ウロカニン酸、ウロカニン酸エチル、2−フェニル−5−メチルベンゾオキサゾール、2−(2'−ヒドロキシ−5'−メチルフェニル)ベンゾトリアゾール、4−tert−ブチル−4'−メトキシジベンゾイルメタン等の紫外線吸収剤を本発明品含有化粧品中に配合することができる。 For example, when the cosmetics containing the present invention is used as a suncare product, benzoic acid-based ultraviolet absorbers such as paraaminobenzoic acid; anthranilic acid-based ultraviolet absorbers such as methyl anthranilate; octyl salicylate, phenyl salicylate, homomentyl salicylate, etc. Salicylic acid UV absorbers: isopropyl paramethoxycinnamate, octyl paramethoxycinnamate, 2-methoxyhexyl paramethoxycinnamate, glyceryl mono-2-ethylhexanoate diparamethoxycinnamate, [4-bis (Trimethylsiloxy) methylsilyl-3-methylbutyl] -3,4,5-trimethoxycinnamic acid ester and other cinnamic acid-based UV absorbers; 2,4-dihydroxybenzophenone, 2-hydroxy-4-methoxybenzophenone, 2 -Hydroxy-4-methoxybe Benzophenone ultraviolet absorbers such as zophenone-5-sulfonic acid, sodium 2-hydroxy-4-methoxybenzophenone-5-sulfonate; urocanic acid, ethyl urocanate, 2-phenyl-5-methylbenzoxazole, 2- (2 Ultraviolet absorbers such as' -hydroxy-5'-methylphenyl) benzotriazole and 4-tert-butyl-4'-methoxydibenzoylmethane can be blended in the cosmetics containing the product of the present invention.
また、保湿効果を本発明品含有化粧品中に付与するために、ポリエチレングリコール、プロピレングリコール、1、3−ブチレングリコール、ヘキシレングリコール、グリセリン、ジグリセリン、キシリトール、マルチトール、マルトース、D−マンニット、水アメ、ブドウ糖、果糖、乳糖、コンドロイチン硫酸ナトリウム、ヒアルロン酸ナトリウム、アデノシンリン酸ナトリウム、乳酸ナトリウム、胆汁酸塩、ピロリドンカルボン酸、グルコサミン、シクロデキストリン等の保湿剤を配合することができる。
さらに薬剤成分として、ビタミンA油、レチノール、パルミチン酸レチノール、イノシット、塩酸ピリドキシン、ニコチン酸ベンジル、ニコチン酸アミド、ニコチン酸dl−α−トコフェロール、アスコルビン酸リン酸マグネシウム、ビタミンD2 (エルゴカルシフェロール)、dl−α−トコフェロール、dl−α−トコフェロール−2−L−アスコルビン酸ジエステルカリウム、酢酸dl−α−トコフェロール、パントテン酸、ビオチン等のビタミン類;エストラジオール、エチニルエストラジオール等のホルモン類;アルギニン、アスパラギン酸、シスチン、システイン、メチオニン、セリン、ロイシン、トリプトファン等のアミノ酸類;アラントイン、アズレン、グリチルレチン酸等の抗炎症剤;アルブチン等の美白剤;酸化亜鉛、タンニン酸等の収斂剤;L−メントール、カンフル等の清涼剤、イオウ、塩化リゾチーム、塩酸ピリドキシン、γ−オリザノール等を配合することができる。 さらに、多様な薬効を有する各種の抽出物を配合することができる。すなわち、ドクダミエキス、オウバクエキス、メリロートエキス、オドリコソウエキス、カンゾウエキス、シャクヤクエキス、サボンソウエキス、ヘチマエキス、キナエキス、ユキノシタエキス、クララエキス、コウホネエキス、ウイキョウエキス、サクラソウエキス、バラエキス、ジオウエキス、レモンエキス、シコンエキス、アロエエキス、ショウブ根エキス、ユーカリエキス、スギナエキス、セージエキス、タイムエキス、茶エキス、海草エキス、キューカンバーエキス、チョウジエキス、キイチゴエキス、メリッサエキス、ニンジンエキス、マロニエエキス、モモエキス、桃葉エキス、クワエキス、ヤグルマギクエキス、ハマメリスエキス、プラセンタエキス、胸腺抽出物、シルク抽出液等を配合することができる。In order to impart a moisturizing effect to the cosmetics containing the present invention, polyethylene glycol, propylene glycol, 1,3-butylene glycol, hexylene glycol, glycerin, diglycerin, xylitol, maltitol, maltose, D-mannitol Moisturizing agents such as water candy, glucose, fructose, lactose, sodium chondroitin sulfate, sodium hyaluronate, sodium adenosine phosphate, sodium lactate, bile salt, pyrrolidone carboxylic acid, glucosamine, cyclodextrin and the like can be blended.
Furthermore, as a pharmaceutical ingredient, vitamin A oil, retinol, retinol palmitate, inosit, pyridoxine hydrochloride, benzyl nicotinate, nicotinamide, nicotinic acid dl-α-tocopherol, magnesium ascorbate phosphate, vitamin D2 (ergocalciferol), vitamins such as dl-α-tocopherol, dl-α-tocopherol-2-L-ascorbic acid potassium ester, dl-α-tocopherol acetate, pantothenic acid and biotin; hormones such as estradiol and ethinylestradiol; arginine and aspartic acid Amino acids such as cystine, cysteine, methionine, serine, leucine and tryptophan; anti-inflammatory agents such as allantoin, azulene and glycyrrhetinic acid; whitening agents such as arbutin; zinc oxide, tan Astringents such as nitric acid; refreshing agents such as L-menthol and camphor, sulfur, lysozyme chloride, pyridoxine hydrochloride, γ-oryzanol and the like can be blended. Furthermore, various extracts having various medicinal effects can be blended. In other words, Dokudami Extract, Oat Extract, Merilot Extract, Oyster Extract, Licorice Extract, Peonies Extract, Soap Extract, Loofah Extract, Kina Extract, Yukinoshita Extract, Clara Extract, Licorice Extract, Fennel Extract, Primrose Extract, Rose Extract, Giant Extract, Lemon Extract , Sicon extract, aloe extract, ginger root extract, eucalyptus extract, horsetail extract, sage extract, thyme extract, tea extract, seaweed extract, cucumber extract, clove extract, raspberry extract, melissa extract, carrot extract, maroni extract, peach extract, peach leaf extract Mulberry extract, cornflower extract, hamamelis extract, placenta extract, thymus extract, silk extract and the like can be blended.
なお、上記した薬効成分に、本発明品含有化粧品中に配合可能な他の薬効成分が限定されるものではない。また、上に挙げた薬効成分は単独で本発明品含有化粧品中に配合することの他に、2種類以上の上記薬効成分を、目的に応じ、適宜組み合わせて配合することも可能である。さらに、上記薬効成分は遊離の状態で使用される他、造塩可能なものは酸又は塩基の塩として、またカルボン酸基を有するものはそのエステルの形で本発明品含有化粧品中に配合することも可能である。
本発明品含有化粧品中は、基礎化粧品であれば、洗顔料、乳液、クリーム、ジェル、エッセンス(美容液)、パック・マスク等の形態に広く適用可能である。また、メーキャップ化粧品であれば、ファンデーション、口紅等の形態に広く適用可能である。そして、これらの形態に、本発明皮膚化粧品の採り得る形態が限定されるものではない。本発明品含有化粧品中においては、これらの所望する形態に応じて通常公知の基剤成分等を、その配合により本発明の所期の効果を損なわない範囲で広く配合して用いることができる。
すなわち、アマニ油、ツバキ油、マカデミアナッツ油、トウモロコシ油、ミンク油、オリーブ油、アボガド油、サザンカ油、ヒマシ油、サフラワー油、キョウニン油、シナモン油、ホホバ油、ブドウ油、ヒマワリ油、アーモンド油、ナタネ油、ゴマ油、小麦胚芽油、米胚芽油、米ヌカ油、綿実油、大豆油、落花生油、茶実油、月見草油、卵黄油、牛脚油、肝油、トリグリセリン、トリオクタン酸グリセリン、トリイソパルミチン酸グリセリン等の液体油脂;ヤシ油、パーム油、パーム核油等の液体又は固体の油脂;カカオ脂、牛脂、羊脂、豚脂、馬脂、硬化油、硬化ヒマシ油、モクロウ、シアバター等の固体油脂;ミツロウ、キャンデリラロウ、綿ロウ、カルナウバロウ、ベイベリーロウ、イボタロウ、鯨ロウ、モンタンロウ、ヌカロウ、ラノリン、還元ラノリン、硬質ラノリン、カポックロウ、サトウキビロウ、ホホバロウ、セラックロウ等のロウ類を本発明品含有化粧品中に配合することができる。In addition, the other medicinal component which can be mix | blended with the above-mentioned medicinal component in the cosmetics containing this invention is not limited. In addition to the above-mentioned medicinal ingredients being blended alone in the cosmetics containing the product of the present invention, two or more kinds of the medicinal ingredients can be blended in appropriate combinations depending on the purpose. Furthermore, the above-mentioned medicinal ingredients are used in a free state, and those capable of salt formation are incorporated into the cosmetics containing the product of the present invention in the form of an acid or base salt and those having a carboxylic acid group in the form of its ester. It is also possible.
In the cosmetics containing the present invention, if it is a basic cosmetic, it can be widely applied to forms such as facial cleansers, milky lotions, creams, gels, essences (beauty serums), packs and masks. In addition, makeup cosmetics can be widely applied to forms such as foundations and lipsticks. And the form which this invention skin cosmetics can take is not limited to these forms. In the cosmetics containing the product of the present invention, conventionally known base components and the like can be widely blended and used in a range that does not impair the desired effect of the present invention by blending them in accordance with these desired forms.
Linseed oil, camellia oil, macadamia nut oil, corn oil, mink oil, olive oil, avocado oil, sasanqua oil, castor oil, safflower oil, kyounin oil, cinnamon oil, jojoba oil, grape oil, sunflower oil, almond oil, Rapeseed oil, sesame oil, wheat germ oil, rice germ oil, rice bran oil, cottonseed oil, soybean oil, peanut oil, tea seed oil, evening primrose oil, egg yolk oil, cow leg oil, liver oil, triglycerin, glyceryl trioctanoate, triiso Liquid fats such as glyceryl palmitate; liquid or solid fats such as coconut oil, palm oil, palm kernel oil; cocoa butter, beef tallow, sheep fat, tallow, horse fat, hydrogenated oil, hydrogenated castor oil, molasses, shea butter Solid fats such as beeswax, candelilla wax, cotton wax, carnauba wax, bayberry wax, ibota wax, whale wax, montan wax, nukarou, la Phosphorus, reduced lanolin, hard lanolin, may be formulated kapok wax, sugarcane wax, jojoba wax, a wax such as shellac wax in the present invention product containing cosmetics.
また、オクタン酸セチル等のオクタン酸エステル、トリ−2−エチルヘキサエン酸グリセリン、テトラ−2−エチルヘキサン酸ペンタエリスリット等のイソオクタン酸エステル、ラウリン酸ヘキシル等のラウリン酸エステル、ミリスチン酸イソプロピル、ミリスチン酸オクチルドデシル等のミリスチン酸エステル、パルミチン酸オクチル等のパルミチン酸エステル、ステアリン酸イソセチル等のステアリン酸エステル、イソステアリン酸イソプロピル等のイソステアリン酸エステル、イソパルミチン酸オクチル等のイソパルミチン酸エステル、オレイン酸イソデシル等のオレイン酸エステル、アジピン酸ジイソプロピル等のアジピン酸ジエステル、セバシン酸ジエチル等のセバシン酸ジエステル、リンゴ酸ジイソステアリル等のエステル油;流動パラフィン、オゾケライト、スクワラン、スクワレン、プリスタン、パラフィン、イソパラフィン、セレシン、ワセリン、マイクロクリスタリンワックス等の炭化水素油を本発明品含有化粧品中に配合することができる。
また、ジメチルポリシロキサン、メチルフェニルポリシロキサン、メチルハイドロジェンポリシロキサン等の鎖状シリコーン、オクタメチルシクロテトラシロキサン、デカメチルシクロペンタシロキサン、ドデカメチルシクロヘキサシロキサン等の環状シリコーン、3次元網目構造を有するシリコーン樹脂、シリコーンゴム等のシリコーンを本発明品含有化粧品中に配合することができる。そして、メタノール、エタノール、プロパノール、イソプロパノール等の低級アルコール;コレステロール、シトステロール、フィトステロール、ラノステロール等のステロール類を本発明品含有化粧品中に配合することができる。また、アラビアゴム、トラガントガム、ガラクタン、キャロブガム、グアーガム、カラヤガム、カラギーナン、ペクチン、寒天、クインスシード(マルメロ)、アルゲコロイド(褐藻エキス)、デンプン(コメ、トウモロコシ、バレイショ、コムギ)等の植物系高分子、デキストラン、サクシノグルカン、プルラン等の微生物系高分子、カルボキシメチルデンプン、メチルヒドロキシプロピルデンプン等のデンプン系高分子、コラーゲン、カゼイン、アルブミン、ゼラチン等の動物系高分子、メチルセルロース、ニトロセルロース、エチルセルロース、メチルヒドロキシプロピルセルロース、ヒドロキシエチルセルロース、セルロース硫酸ナトリウム、ヒドロキシプロピルセルロース、カルボキシメチルセルロースナトリウム、結晶セルロース、セルロース末等のセルロース系高分子、アルギン酸ナトリウム、アルギン酸プロピレングリコールエステル等のアルギン酸系高分子、ポリビニルメチルエーテル、カルボキシビニルポリマー(CARBOPOL等)等のビニル系高分子、ポリオキシエチレン系高分子、ポリオキシエチレンポリオキシプロピレン共重合体系高分子、ポリアクリル酸ナトリウム、ポリエチルアクリレート、ポリアクリル酸アミド等のアクリル系高分子、ポリエチレンイミン、カチオンポリマー、ベントナイト、ケイ酸アルミニウムマグネシウム、ラポナイト、ヘクトライト、無水ケイ酸等の無機系水溶性高分子等の水溶性高分子を本発明品含有化粧品中に配合することができる。Also, octanoic acid esters such as cetyl octanoate, glycerin tri-2-ethylhexanoate, isooctanoic acid esters such as tetra-2-ethylhexanoic acid pentaerythritol, lauric acid esters such as hexyl laurate, isopropyl myristate, Myristic acid ester such as octyldodecyl myristate, palmitic acid ester such as octyl palmitate, stearic acid ester such as isocetyl stearate, isostearic acid ester such as isopropyl isostearate, isopalmitic acid ester such as octyl isopalmitate, oleic acid Oleic acid esters such as isodecyl; adipic acid diesters such as diisopropyl adipate; sebacic acid diesters such as diethyl sebacate; ester oils such as diisostearyl malate; Dynamic paraffin may be blended ozokerite, squalane, squalene, pristane, paraffin, isoparaffin, ceresin, vaseline, hydrocarbon oils such as microcrystalline wax in the present invention product containing cosmetics.
It also has a chain silicone such as dimethylpolysiloxane, methylphenylpolysiloxane, and methylhydrogenpolysiloxane, a cyclic silicone such as octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane, and dodecamethylcyclohexasiloxane, and a three-dimensional network structure. Silicone such as silicone resin and silicone rubber can be blended in the cosmetics containing the product of the present invention. And lower alcohols, such as methanol, ethanol, propanol, and isopropanol; Sterols, such as cholesterol, sitosterol, phytosterol, and lanosterol, can be mix | blended in this invention containing cosmetics. In addition, plant polymers such as gum arabic, gum tragacanth, galactan, carob gum, guar gum, caraya gum, carrageenan, pectin, agar, quince seed (quince), alge colloid (brown algae extract), starch (rice, corn, potato, wheat) Microbial polymers such as dextran, succinoglucan and pullulan, starch polymers such as carboxymethyl starch and methylhydroxypropyl starch, animal polymers such as collagen, casein, albumin and gelatin, methylcellulose, nitrocellulose and ethylcellulose , Methyl hydroxypropyl cellulose, hydroxyethyl cellulose, cellulose sodium sulfate, hydroxypropyl cellulose, carboxymethyl cellulose sodium, crystal cellulose Cellulose polymers such as cellulose powder, alginic acid polymers such as sodium alginate and propylene glycol alginate, vinyl polymers such as polyvinyl methyl ether and carboxyvinyl polymer (such as CARBOPOL), polyoxyethylene polymers, poly Oxyethylene polyoxypropylene copolymer polymer, acrylic polymer such as sodium polyacrylate, polyethyl acrylate, polyacrylamide, polyethylenimine, cationic polymer, bentonite, magnesium aluminum silicate, laponite, hectorite, anhydrous Water-soluble polymers such as inorganic water-soluble polymers such as silicic acid can be blended in the cosmetics containing the product of the present invention.
さらに、アラニン、エデト酸ナトリウム塩、ポリリン酸ナトリウム、メタリン酸ナトリウム、リン酸等の金属イオン封鎖剤;2−アミノ−2−メチル−1−プロパノール、2−アミノ−2−メチル−1、3−プロパンジオール、水酸化カリウム、水酸化ナトリウム、L−アルギニン、L−リジン、トリエタノールアミン、炭酸ナトリウム等の中和剤;乳酸、クエン酸、グリコール酸、コハク酸、酒石酸、dl−リンゴ酸、炭酸カリウム、炭酸水素ナトリウム、炭酸水素アンモニウム等のpH調整剤;アスコルビン酸、α−トコフェロール、ジブチルヒドロキシトルエン、ブチルヒドロキシアニソール等の酸化防止剤を本発明品含有化粧品中に配合することができる。
また、安息香酸、サリチル酸、石炭酸、ソルビン酸、パラオキシ安息香酸エステル、パラクロルメタクレゾール、ヘキサクロロフェン、塩化ベンザルコニウム、塩化クロルヘキシジン、トリクロロカルバニリド、感光素、フェノキシエタノール等の抗菌剤等を本発明品含有化粧品中に配合することができる。また、必要に応じて適当な香料、色素等を本発明の所期の効果を損なわない範囲で本発明品含有化粧品中に配合することもできる。
なお、本発明品含有化粧品中の安定性のさらなる向上を図るために、少量の界面活性剤、例えばモノグリセライド,ソルビタン脂肪酸エステル,ポリグリセリン脂肪酸エステル,ポリオキシエチレン硬化ヒマシ油,ポリオキシエチレン脂肪酸エーテル等を本発明品含有化粧品中に配合することができる。ここで、上記の基剤成分は例示であり、これらの基剤成分に本発明品含有化粧品中に配合可能な基剤成分が限定されるものではない。これらの基剤成分は所望する形態に応じた処方に従い、適宜組み合わせて本発明品含有化粧品中に配合することができる。本発明品含有化粧品中の具体的処方については、後述する実施例において記載する。Further, sequestering agents such as alanine, sodium edetate, sodium polyphosphate, sodium metaphosphate, phosphoric acid; 2-amino-2-methyl-1-propanol, 2-amino-2-methyl-1, 3- Neutralizing agents such as propanediol, potassium hydroxide, sodium hydroxide, L-arginine, L-lysine, triethanolamine, sodium carbonate; lactic acid, citric acid, glycolic acid, succinic acid, tartaric acid, dl-malic acid, carbonic acid A pH adjuster such as potassium, sodium hydrogen carbonate or ammonium hydrogen carbonate; an antioxidant such as ascorbic acid, α-tocopherol, dibutylhydroxytoluene or butylhydroxyanisole can be incorporated into the cosmetics containing the product of the present invention.
In addition, the present invention includes antibacterial agents such as benzoic acid, salicylic acid, coalic acid, sorbic acid, paraoxybenzoic acid ester, parachlorometacresol, hexachlorophene, benzalkonium chloride, chlorhexidine chloride, trichlorocarbanilide, photosensitizer, and phenoxyethanol. It can mix | blend in goods containing cosmetics. Further, if necessary, suitable perfumes, pigments and the like can be blended in the cosmetics containing the product of the present invention as long as the intended effects of the present invention are not impaired.
In order to further improve the stability in the cosmetics containing the product of the present invention, a small amount of a surfactant such as monoglyceride, sorbitan fatty acid ester, polyglycerin fatty acid ester, polyoxyethylene hydrogenated castor oil, polyoxyethylene fatty acid ether, etc. Can be blended in the cosmetics containing the product of the present invention. Here, the above-described base components are exemplifications, and the base components that can be blended in the cosmetics containing the product of the present invention are not limited to these base components. These base components can be appropriately combined and blended in the cosmetics according to the present invention in accordance with a prescription according to a desired form. Specific prescriptions in the cosmetics containing the product of the present invention will be described in Examples described later.
このように、チアシードからチア種子とチア種子外殻多糖類を物理的、工業的レベルで分離できる。また、本発明によって提供される外殻粘性多糖類は、チアシードに化学処理を施していないため、変性などは起こしておらず、種子成分が含まれない粘性、保水性の高い多糖類である。
すなわち、チアシードからチアシードの外殻粘性多糖類と、種子本体・内部の組成物である脂質、たんぱく質、灰分、食物繊維多糖類とを分離して提供することが可能となり、食品、化粧品素材としての応用範囲が広がる。In this way, chia seeds and chia seed shell polysaccharides can be separated from chia seeds at a physical and industrial level. In addition, the outer-shell viscous polysaccharide provided by the present invention is a polysaccharide with high viscosity and high water retention that does not contain denaturation and does not contain seed components because the chia seeds are not chemically treated.
That is, it is possible to separate and provide the chia seed shell polysaccharide from the chia seed and the seed body / internal composition lipid, protein, ash, and dietary fiber polysaccharide. The range of application is expanded.
次に、本発明の実施形態について、図表を参照しつつ説明するが、本発明の技術的範囲は、これらの実施形態によって限定されるものではなく、発明の要旨を変更することなく様々な形態で実施することができる。
<実施例1:チアシードの種子及び種子以外の組成物の作製>
チアシードに5〜50倍量の水を加え、数時間〜一夜漬し、時々攪拌するか又は常時ゆるやかな攪拌を行った。
浸漬に使用する水の量としては、5倍以下では種子表面の多糖類の膨潤が不十分で種子に傷を付けずに分離することが困難となるので好ましくない。また、50倍以上では浸潤液が希薄となり、分離処理時間が長くなり、均質な多糖類の分離が困難になると共に、以後の濃縮工程が長くなるので好ましくない。
攪拌の回転数は、500rpm〜10000rpmが好ましい。
チアシードが給水して多糖類が膨潤すると、粘性が高くなるので、攪拌回転数が500rpm以下では攪拌も困難で多糖類も分離できなくなる。また、10000rpm以上の回転数では処理時間は短縮されるが、種子外殻に傷が付き易く、種子成分、特に種子外殻の褐色色素性成分などが混入し、異臭が強くなる。
攪拌羽又はローターと攪拌機外壁とのクリアランスは、1mm〜100mmが好ましい。
クリアランスが、1mm以下になると種子が破壊されるため、適切ではない。また、100mm以上では、多糖類の分離に時間を要し、種子本体の成分が混入し、均質な多糖類の分離が困難になる。
本明細書において、チアシードを遠心して得られた沈殿側を種子(チアシード種子)と、それ以外の部分をチア外殻多糖類(本件組成物)と称する。Next, embodiments of the present invention will be described with reference to the drawings. However, the technical scope of the present invention is not limited by these embodiments, and various forms can be made without changing the gist of the invention. Can be implemented.
<Example 1: Preparation of chia seeds and compositions other than seeds>
5 to 50 times the amount of water was added to the chia seeds, soaked for several hours to overnight, and occasionally stirred or always gently stirred.
If the amount of water used for the dipping is 5 times or less, it is not preferable because the polysaccharide on the seed surface is insufficiently swollen and it is difficult to separate the seed without damaging it. On the other hand, if it is 50 times or more, the infiltrating solution becomes dilute, the separation time becomes long, it becomes difficult to separate homogeneous polysaccharides, and the subsequent concentration step becomes long, which is not preferable.
The rotation speed of stirring is preferably 500 rpm to 10,000 rpm.
When the chia seed is supplied with water and the polysaccharide swells, the viscosity increases. Therefore, stirring is difficult at a rotation speed of 500 rpm or less, and the polysaccharide cannot be separated. In addition, at a rotational speed of 10,000 rpm or more, the treatment time is shortened, but the seed shell is easily damaged, seed components, particularly brown pigment components in the seed shell, and the like, and the off-flavor becomes strong.
The clearance between the stirring blade or rotor and the outer wall of the stirrer is preferably 1 mm to 100 mm.
If the clearance is 1mm or less, seeds are destroyed, which is not appropriate. On the other hand, when the length is 100 mm or more, it takes time to separate the polysaccharide, and the components of the seed body are mixed, making it difficult to separate the homogeneous polysaccharide.
In the present specification, the precipitation side obtained by centrifuging chia seeds is referred to as seeds (chia seeds), and the other part is referred to as chia shell polysaccharide (the present composition).
<実施例2:回転数による粘度の相違>
次に、チアシードの種子以外の組成物であるチア外殻多糖類について、回転数の変化による粘度の相違を調べた。
粘度は、各濃度とも蒸留水に既定量のチア外殻多糖類を攪拌投入し、25℃で2時間攪拌溶解し、一夜例保存後、B型粘度計を用い、25℃、各回転数(6rpm、 12rpm、 30rpm、 60rpm)で測定した。
結果を表1に示した。<Example 2: Viscosity difference depending on rotational speed>
Next, for the chia shell polysaccharide, which is a composition other than the seeds of chia seeds, the difference in viscosity due to the change in the rotational speed was examined.
Viscosity is determined by adding a predetermined amount of thia-shell polysaccharide into distilled water with stirring and dissolving at 25 ° C for 2 hours, storing overnight, and then using a B-type viscometer at 25 ° C at each rotation speed ( 6 rpm, 12 rpm, 30 rpm, 60 rpm).
The results are shown in Table 1.
<実施例3:チア外殻多糖類の成分>
分析項目として、多糖類、脂質、蛋白質及び灰分の4項目を選択し、本件組成物の成分を調べた。分析結果を表2に示した。
表に示す通り、本件組成物は、チア種子に比べると、蛋白含量及び脂質含量が大幅に低減し、高度に多糖類を含有していた。このように、チア外殻から特異的な多糖類を得ることに成功した。<Example 3: Ingredients of thia outer polysaccharide>
As analysis items, four items of polysaccharide, lipid, protein, and ash were selected, and the components of the composition were examined. The analysis results are shown in Table 2.
As shown in the table, the present composition was significantly reduced in protein content and lipid content as compared with chia seeds, and highly contained polysaccharides. Thus, it succeeded in obtaining a specific polysaccharide from a thia shell.
<実施例4:加水量>
チアシードに質量比で2〜50倍量の水を加え、3時間漬し、時々攪拌するか又は常時ゆるやかな攪拌を行った。その後、回転数を4500rpm、攪拌羽と攪拌機外壁間の距離(クリアランス)を50mmに設定して、攪拌した。
得られた本件組成物の結果を表3に示した。<Example 4: Amount of water added>
2 to 50 times the amount of water was added to the chia seeds, soaked for 3 hours, and stirred occasionally or constantly gently. Thereafter, the number of revolutions was set to 4500 rpm, and the distance (clearance) between the stirring blade and the outer wall of the stirrer was set to 50 mm, followed by stirring.
The results of the composition obtained are shown in Table 3.
<実施例5:回転数>
チアシードに質量比で20倍量の水を加え、3時間漬し、時々攪拌するか又は常時ゆるやかな攪拌を行った。その後、回転数を500rpm〜10000rpmの範囲で設定し、攪拌羽と攪拌機外壁間の距離(クリアランス)は50mmに設定して攪拌した。
得られた本件組成物の結果を表4に示した。<Example 5: Number of rotations>
A 20-fold amount of water was added to the chia seed in a mass ratio, soaked for 3 hours, and stirred occasionally or constantly gently. Thereafter, the number of revolutions was set in the range of 500 rpm to 10,000 rpm, and the distance (clearance) between the stirring blade and the outer wall of the stirrer was set to 50 mm and stirred.
The results of the composition obtained are shown in Table 4.
給水して多糖類が膨潤したチアシードの粘性は高いため、攪拌回転数が500rpm以下では攪拌も困難で多糖類は分離困難であった。
また、10000rpm以上の回転数では処理時間は短縮されるが、種子外殻に傷が付き易く、種子成分、特に種子外殻の褐色色素性成分などが混入し、異臭が出た。
このため、攪拌の回転数は、500rpm〜10000rpmが好ましいことが分かった。Since the viscosity of chia seeds in which the polysaccharide was swollen with water supply was high, stirring was difficult at a rotation speed of 500 rpm or less, and the polysaccharide was difficult to separate.
In addition, at a rotational speed of 10,000 rpm or more, the treatment time is shortened, but the seed shell is easily damaged, and seed components, particularly brown pigment components of the seed shell, are mixed, resulting in a strange odor.
For this reason, it turned out that the rotation speed of stirring is preferable 500 rpm-10000 rpm.
<実施例6:クリアランス(攪拌羽と外壁間の距離)>
チアシードに質量比で20倍量の水を加え、3時間漬し、時々攪拌するか又は常時ゆるやかな攪拌を行った。その後、回転数を4500rpmに設定し、攪拌羽と攪拌機外壁間の距離(クリアランス)は0.5mm〜200mmに設定して攪拌した。結果を表5に示した。<Example 6: Clearance (distance between stirring blade and outer wall)>
A 20-fold amount of water was added to the chia seed in a mass ratio, soaked for 3 hours, and stirred occasionally or constantly gently. Thereafter, the number of rotations was set to 4500 rpm, and the distance (clearance) between the stirring blade and the outer wall of the stirrer was set to 0.5 mm to 200 mm and stirred. The results are shown in Table 5.
攪拌羽又はローターと攪拌機外壁とのクリアランスは、1mm以下では種子が破壊されるため、適切ではない。
また、100mm以上では、多糖類の分離に時間を要し、種子本体の成分が混入し易くなり、均質な多糖類の分離が困難になるので、適切ではない。
この結果、クリアランスは、1mm〜100mmが適切であることが分かった。The clearance between the stirring blade or rotor and the outer wall of the stirrer is less than 1 mm because seeds are destroyed, which is not appropriate.
On the other hand, when the length is 100 mm or more, it takes time to separate the polysaccharide, the components of the seed body are likely to be mixed, and it is difficult to separate the homogeneous polysaccharide.
As a result, it was found that a clearance of 1 to 100 mm was appropriate.
<実施例7:アルカリ処理>
次に、チアシード種子をpH9〜pH13のアルカリ水溶液で処理し、チア種子外殻多糖類とチア種子とに分離できるかどうかを調べた。コントロールとして、pH7の水溶液を用いた。結果を表6に示した。<Example 7: Alkali treatment>
Next, the chia seeds were treated with an alkaline aqueous solution of pH 9 to pH 13 to examine whether or not they could be separated into chia seed shell polysaccharides and chia seeds. A pH 7 aqueous solution was used as a control. The results are shown in Table 6.
表に示すように、pH13付近で処理した場合にのみ、種子外殻多糖類が分離した。
次に、pH13で24時間及び48時間アルカリ処理後、種子を遠心分離(3000rpm、10min)し、水溶性成分を凍結乾燥後、乾燥物の粘度を調べた。
粘度は、蒸留水に1質量%の上記乾燥物(チア外殻多糖類)を攪拌投入し、25℃で2時間攪拌溶解し、一夜冷蔵保存後、B型粘度計を用い、25℃、各回転数(6rpm、 12rpm、 30rpm、 60rpm)で測定した。
結果を表7に示した。As shown in the table, seed shell polysaccharides were separated only when treated at around pH 13.
Next, after alkali treatment at pH 13 for 24 hours and 48 hours, the seed was centrifuged (3000 rpm, 10 min), the water-soluble component was freeze-dried, and the viscosity of the dried product was examined.
Viscosity is as follows: 1% by mass of the above dried product (thia shell polysaccharide) is stirred into distilled water, stirred and dissolved at 25 ° C. for 2 hours, and stored overnight at 25 ° C. using a B-type viscometer. Measured at the number of rotations (6 rpm, 12 rpm, 30 rpm, 60 rpm).
The results are shown in Table 7.
<実施例8:透明度>
本件組成物の0.1%及び1%の水溶液を作製し、660nmの波長でABS値を測定した。
その結果、0.1%濃度で0.008以下(透明)であり、1%濃度で0.200-0.500の値を示した。
<実施例9:保水量>
本件組成物1gに水30gを加え、3時間、時々攪拌するか又は常時ゆるやかな攪拌を行った。
ポリエチレン製濾戸に濾紙を密着させ、含水させた本件組成物を濾紙上に加え、1min静置後、質量を測定した。
この試験法による、保水量は本件組成物1g当たり、10g〜20gであった。<Example 8: Transparency>
0.1% and 1% aqueous solutions of the composition were prepared, and ABS values were measured at a wavelength of 660 nm.
As a result, it was 0.008 or less (transparent) at 0.1% concentration, and a value of 0.200-0.500 at 1% concentration.
<Example 9: Water retention amount>
30 g of water was added to 1 g of the present composition, and stirred occasionally for 3 hours, or constantly gently stirred.
The filter paper was brought into close contact with a polyethylene filter door, the water-containing composition was added onto the filter paper, allowed to stand for 1 min, and then mass was measured.
The amount of water retained by this test method was 10 to 20 g per 1 g of the present composition.
<実施例10:分子量の分布>
(1)本件組成物の分子量分布を測定した。分子量の測定には、光速液体クロマトグラフィー(HPLC)の分離モードの一つであるサイズ排除クロマトグラフィーを用いた。
その結果、本件組成物の多糖類の分子量は、10000(1×104)〜10000000(1×107)であることが分かった。
(2)本件組成物(チア外殻多糖類)を3000rpm以上で10min〜30min遠心分離すると、多糖類は上層と下層の2層に分離した。上層及び下層を分取した様子を図1に示した。
上層成分は、粘性は無いが、皮膚に塗布した際のすべり感が良好であった。サイズ排除クロマトグラフィーにより、チア外殻多糖類の上層の分子量分布を測定した。その結果、上層多糖類の分子量は、5000(5×103)〜10000(1×104)であった。上層成分については、特に化粧品への応用が良好であると考えられた。
また、下層成分は、粘性が大きかった。サイズ排除クロマトグラフィーにより、下層の分子量分布を測定した結果、10000(1×104)〜10000000(1×107)であった。<Example 10: Molecular weight distribution>
(1) The molecular weight distribution of the composition was measured. For the measurement of molecular weight, size exclusion chromatography, which is one of the separation modes of light-speed liquid chromatography (HPLC), was used.
As a result, the molecular weight of the polysaccharide of the present composition was found to be 10000 (1 × 10 4 ) to 10000000 (1 × 10 7 ).
(2) When this composition (thia shell polysaccharide) was centrifuged at 3000 rpm or more for 10 min to 30 min, the polysaccharide was separated into two layers, an upper layer and a lower layer. A state in which the upper layer and the lower layer are separated is shown in FIG.
The upper layer component was not viscous, but had a good feeling of slip when applied to the skin. The molecular weight distribution of the upper layer of thia-shell polysaccharide was measured by size exclusion chromatography. As a result, the molecular weight of the upper polysaccharide was 5000 (5 × 10 3 ) to 10000 (1 × 10 4 ). The upper layer component was considered to be particularly well applied to cosmetics.
Moreover, the lower layer component had a large viscosity. As a result of measuring the molecular weight distribution of the lower layer by size exclusion chromatography, it was 10000 (1 × 10 4 ) to 10000000 (1 × 10 7 ).
<実施例11:種子からの油脂の抽出>
種子外殻表面の粘質多糖類を除去した種子から油脂成分を圧搾ろ過抽出した場合、多糖類を除去する前の種子に比べ、抽出率が5〜20%増加した。
<実施例12:食品(食パン)への応用>
本発明によって得られた本件組成物を用いて食パンを作製した。表8に記す配合と割合で、強力粉、ドライイースト、上白糖、食塩、脱脂粉乳、ショートニング、水を加え、本発明品及び比較品としてのチアシードを同量添加したもの並びに無添加のものを準備し、自動ホームベーカリーを用いて、練り・ねかし・発酵・焼成の合計が3時間にて山形食パンを作製した。
その後、得られた食パンをやわからさ、しっとり感、もちもち感の三点で官能評価し、無添加品を1点とし、最高点を10点として、評価点数が高い程良い評価とした。パネラー20名を用いて、食したときの評価を求めた。結果を表8に示した。<Example 11: Extraction of fats and oils from seeds>
When the oil and fat component was extracted by pressure filtration from the seed from which the viscous polysaccharide on the seed shell surface was removed, the extraction rate increased by 5 to 20% compared to the seed before removing the polysaccharide.
<Example 12: Application to food (bread)>
A bread was prepared using the present composition obtained according to the present invention. Prepared with the addition and addition of strong powder, dry yeast, white saccharose, salt, skim milk powder, shortening, water and the same amount of the present invention and the chia seed as a comparative product in the composition and ratio shown in Table 8 Then, using an automatic home bakery, Yamagata bread was prepared in 3 hours, including kneading, cooking, fermentation and baking.
Thereafter, the bread bread obtained was sensory-evaluated with three points of ease of understanding, moist feeling, and glutinous feeling, the additive-free product was assigned 1 point, the highest point was 10 points, and the higher the evaluation score, the better the evaluation. 20 panelists were used to evaluate when they ate. The results are shown in Table 8.
<実施例13:麺類への応用>
中力小麦粉100に対して水45、食塩5を配合し、常法によりうどんを製造した。配合時に本件組成物を1の割合で配合した。
うどんは、ほぐれ制、弾力、腰、つるみ感の4点で官能評価し、無添加品と比較した。
評価基準は、1:良くない、2:あまり良くない、3:普通、4:良い、5:非常に良い、の5段階とし、パネラー20名で評価した。結果を表9に示した。<Example 13: Application to noodles>
Udon was produced in a conventional manner by adding water 45 and salt 5 to medium strength flour 100. The present composition was blended at a ratio of 1 at the time of blending.
Udon was sensory-evaluated with four points: looseness, elasticity, waist, and sag, and compared with additive-free products.
The evaluation criteria were five levels: 1: not good, 2: not good, 3: normal, 4: good, 5: very good, and evaluated by 20 panelists. The results are shown in Table 9.
<実施例14>
本発明によって得られたチア外殻多糖類(前記組成物)を用いてシャーベットを作製した。表10に記す配合と割合で桃(生果実)、ヨーグルト、牛乳、砂糖、生クリーム、本発明品及び比較品としてのチアシードを同量添加したもの並びに無添加のものを準備し、ミキサーを用いて混合粉砕し、-50℃で急速冷凍した。その後、-10℃の家庭用冷蔵庫にて1日保管し、評価を実施した。
その後、得られたシャーベットを口解け易さ、果肉感の二点で官能評価し、無添加品を1とし、最高点を10点として、評価点数が高い程良い評価とした。パネラー20名を用いて、食したときの評価を求めた。結果を表10に示した。<Example 14>
A sherbet was prepared using the thia outer polysaccharide (the composition) obtained according to the present invention. Prepare peach (raw fruit), yogurt, milk, sugar, fresh cream, the present invention product and the same amount of chia seed as a comparison product, and the additive-free product with the composition and ratio shown in Table 10, and use a mixer. The mixture was pulverized and rapidly frozen at -50 ° C. Thereafter, it was stored in a household refrigerator at -10 ° C for 1 day and evaluated.
Thereafter, the obtained sherbet was subjected to sensory evaluation with two points of ease of mouthbreaking and fleshiness, the additive-free product was set to 1, the highest score was 10 points, and the higher the evaluation score, the better the evaluation. 20 panelists were used to evaluate when they ate. The results are shown in Table 10.
表に示す通り、本発明品であるチアシード外殻多糖類を配合したものは、比較品に比べ、口解け易さ、果肉感が上昇しており、シャーベットとして好ましい食感を作ることに成功した。
<実施例15>
本件組成物を0.5質量%、市販清涼飲料に溶解した。
適度な粘度を有する飲料となったが、ベトツキ感は無く、喉越し感の良い飲料を作製することができた。As shown in the table, blended with the chia seed shell polysaccharide, which is the product of the present invention, has improved ease of mouthbreaking and fleshiness compared to the comparative product, and succeeded in creating a favorable texture as a sherbet. .
<Example 15>
This composition was dissolved in 0.5% by mass of a commercial soft drink.
Although the beverage had an appropriate viscosity, there was no stickiness and a beverage with a good feeling over the throat could be produced.
<実施例16>
本件組成物を1.0質量%、市販の醤油に溶解した。
この濃度で、醤油の風味などに影響は無かった。
適度なとろみを付与することで、より少ない量で、醤油の風味を食材に与え、塩分なども減らすことができた。
<実施例17>
本件組成物を0.1〜1.0質量%飲料水に溶解した。
この濃度で、一般に病院・介護施設で使用されるとろみの程度20mPa・s〜500mPa・s(B型粘度計、12rpm)の粘度を達成することができた。
粘度はとろみ剤が使用される温度25度〜70度また、飲料水の風味には影響を与えなかった。<Example 16>
This composition was dissolved in 1.0% by mass of commercially available soy sauce.
This concentration had no effect on the flavor of soy sauce.
By adding a proper thickening, the amount of soy sauce was given to the ingredients in a smaller amount, and the salt content could be reduced.
<Example 17>
This composition was melt | dissolved in 0.1-1.0 mass% drinking water.
At this concentration, it was possible to achieve viscosities of 20 mPa · s to 500 mPa · s (B-type viscometer, 12 rpm), which are generally used in hospitals and nursing homes.
Viscosity did not affect the flavor of drinking water.
<実施例18:化粧品官能評価テスト>
本発明方法によって得られたChia seed(シソ科種子)の外殻多糖類乾燥品と市場品である高品質マルメロ種子抽出物乾燥品の0.1%水溶液を調整した。他の成分の影響を考慮し、水溶液は被検物と精製水で調整した。
25〜60歳(平均年齢43.0)の男女(各20名)を対象に、それぞれの水溶液0.1mlを左右の手の甲に単回塗布するパネルテストを実施した。
被検者には塗布する被検物の内容は知らせないシングルブラインド試験を実施した。結果を表11に示した。<Example 18: Cosmetic sensory evaluation test>
A 0.1% aqueous solution of a dried product of the outer shell polysaccharide of Chia seed (Lamiaceae seed) obtained by the method of the present invention and a dried product of high quality quince seed extract as a marketed product was prepared. Considering the influence of other components, the aqueous solution was adjusted with the test substance and purified water.
A panel test was performed on males and females (20 people each) between 25 and 60 years old (average age 43.0) by applying 0.1 ml of each aqueous solution to the back of each hand.
A single blind test was conducted in which the subject was not informed of the contents of the test object to be applied. The results are shown in Table 11.
表に示す通り、本件組成物は、市場品である高品質マルメロ種子抽出物に比べ、異臭、べたつき、すべり、滑らかさ、しっとり感において良好な結果が得られた。
また、本件組成物は、日焼け止めなどを目的とする皮膚用クリームなど皮膚用化粧品にも応用できる。加えて、洗顔剤、ボディーシャンプーなどで、保湿感、すべり感を付与する目的にも応用できる。
このように本実施形態によれば、チアシードからチア種子とチア種子外殻多糖類を物理的、工業的レベルで分離できた。本実施形態によって提供される外殻粘性多糖類は、チアシードに化学処理を施していないため、変性などは起こしておらず、種子成分が含まれない粘性、保水性の高い多糖類であった。As shown in the table, the present composition gave favorable results in the off-flavor, stickiness, slip, smoothness and moist feeling compared to the marketed high quality quince seed extract.
The present composition can also be applied to skin cosmetics such as a skin cream for sunscreen. In addition, it can be applied for the purpose of imparting moisturizing and slipping feeling with facial cleansers and body shampoos.
Thus, according to this embodiment, chia seeds and chia seed shell polysaccharides could be separated from chia seeds at a physical and industrial level. The outer-shell viscous polysaccharide provided by the present embodiment is a polysaccharide with high viscosity and high water retention that does not contain seed components because no chemical treatment is applied to chia seeds.
次に、本発明品であるチアシード由来組成物を化粧品として実施した。
<実施例19>
本発明品を乳液に応用した。
質量%
A.油相
スクワラン 10.0
パルミチン酸イソプロピル 5.0
ワセリン 3.0
ジメチルポリシロキサン 2.0
ヘキシルデカノール 3.0
α−トコフェロール 0.3
B.水相
トリエタノールアミン 0.25
ポリエチレングリコール 8.0
パラオキシ安息香酸メチル 0.1
メタリン酸ナトリウム 0.1
本発明品 1.2
ヒドロキシプロピルメチルセルロース 0.1
イオン交換水 残 余
(製法)上記油相成分A及び水相成分Bをそれぞれ70℃で溶解し、この油相成分Aを水相成分Bに添加して乳化機で乳化し、この乳化物を攪拌しながら室温まで冷却して、所望する乳液を得た。Next, the chia seed-derived composition which is the product of the present invention was implemented as a cosmetic.
<Example 19>
The product of the present invention was applied to an emulsion.
mass%
A. Oil phase Squalane 10.0
Isopropyl palmitate 5.0
Vaseline 3.0
Dimethylpolysiloxane 2.0
Hexyldecanol 3.0
α-Tocopherol 0.3
B. Aqueous phase Triethanolamine 0.25
Polyethylene glycol 8.0
Methyl paraoxybenzoate 0.1
Sodium metaphosphate 0.1
Product of the present invention 1.2
Hydroxypropyl methylcellulose 0.1
Residue of ion-exchanged water (Manufacturing method) The oil phase component A and the water phase component B are each dissolved at 70 ° C., the oil phase component A is added to the water phase component B and emulsified with an emulsifier. Cool to room temperature with stirring to give the desired emulsion.
<実施例20>
本発明品をクリームに応用した。
質量%
A.油相
デシルテトラデカノール 0.2
オリーブ油 10.0
ラノリン 3.0
トリ2−エチルヘキサン酸グリセリル 3.0
パラメトキシケイ皮酸2−エチルヘキシル 2.0
酢酸dl−α−トコフェロール 0.5
パラオキシ安息香酸エチル 0.1
B.水相
プロピレングリコール 5.0
ヒアルロン酸ナトリウム 0.1
エデト酸三ナトリウム 0.1
PEMULEN TR−2 6.0
カルボキシメチルセルロース 0.8
水酸化カリウム 2.5
本発明品 3.0
イオン交換水 残 余
(製法)上記油相成分A及び水相成分Bをそれぞれ70℃で溶解し、この油相成分Aを水相成分Bに添加して乳化機で乳化して、この乳化物を攪拌して室温まで冷却して、所望するクリームを得た。<Example 20>
The product of the present invention was applied to a cream.
mass%
A. Oil phase Decyltetradecanol 0.2
Olive oil 10.0
Lanolin 3.0
Glyceryl tri-2-ethylhexanoate 3.0
2-Ethylhexyl paramethoxycinnamate 2.0
Dl-α-tocopherol acetate 0.5
Ethyl paraoxybenzoate 0.1
B. Aqueous phase Propylene glycol 5.0
Sodium hyaluronate 0.1
Edetate trisodium 0.1
PEMULEN TR-2 6.0
Carboxymethylcellulose 0.8
Potassium hydroxide 2.5
Product of the present invention 3.0
Residue of ion-exchanged water (Manufacturing method) The oil phase component A and the water phase component B are each dissolved at 70 ° C., and the oil phase component A is added to the water phase component B and emulsified with an emulsifier. Was stirred and cooled to room temperature to give the desired cream.
<実施例21>
本発明品を乳液に応用した。
質量%
A.油相
流動パラフィン 10.0
ホホバ油 4.0
オレイルアルコール 8.0
2−エチルヘキサン酸セチル 3.0
ビタミンA油 0.1
B.水相
アルブチン 2.0
アスコルビン酸リン酸マグネシウム 1.0
プラセンタエキス 0.5
ヘチマエキス 2.0
PEMULEN TR−1 0.02
CARBOPOL 941 0.15
2−アミノ−2−メチル−1−プロパノール 0.3
エデト酢酸ナトリウム 0.15
パラオキシ安息香酸メチル 0.1
フェノキシエタノール 0.2
本発明品 0.3
イオン交換水 残 余
(製法)上記油相成分A及び水相成分Bをそれぞれ70℃で溶解し、この油相成分Aを水相成分Bに添加して乳化機で乳化して、攪拌しながら室温まで冷却して、所望する乳液を得た。<Example 21>
The product of the present invention was applied to an emulsion.
mass%
A. Oil phase Liquid paraffin 10.0
Jojoba oil 4.0
Oleyl alcohol 8.0
Cetyl 2-ethylhexanoate 3.0
Vitamin A oil 0.1
B. Aqueous phase Arbutin 2.0
Magnesium ascorbate phosphate 1.0
Placenta extract 0.5
Loofah extract 2.0
PEMULEN TR-1 0.02
CARBOPOL 941 0.15
2-Amino-2-methyl-1-propanol 0.3
Sodium edetacetate 0.15
Methyl paraoxybenzoate 0.1
Phenoxyethanol 0.2
Product of the present invention 0.3
Residue of ion-exchanged water (Manufacturing method) The oil phase component A and the water phase component B are dissolved at 70 ° C., the oil phase component A is added to the water phase component B, emulsified with an emulsifier, and stirred. Cool to room temperature to obtain the desired emulsion.
<実施例22>
本発明品を乳液に応用した。
質量%
A.油相
スクワラン 10.0
パルミチン酸イソプロピル 5.0
ワセリン 3.0
ジメチルポリシロキサン 2.0
ヘキシルデカノール 3.0
α−トコフェロール 0.3
B.水相
トリエタノールアミン 0.25
ポリエチレングリコール 8.0
パラオキシ安息香酸メチル 0.1
メタリン酸ナトリウム 0.1
本発明品 3.53
ヒドロキシプロピルメチルセルロース 0.1
イオン交換水 残 余<Example 22>
The product of the present invention was applied to an emulsion.
mass%
A. Oil phase Squalane 10.0
Isopropyl palmitate 5.0
Vaseline 3.0
Dimethylpolysiloxane 2.0
Hexyldecanol 3.0
α-Tocopherol 0.3
B. Aqueous phase Triethanolamine 0.25
Polyethylene glycol 8.0
Methyl paraoxybenzoate 0.1
Sodium metaphosphate 0.1
Invention product 3.53
Hydroxypropyl methylcellulose 0.1
Ion exchange water
(製法)上記油相成分A及び水相成分Bをそれぞれ70℃で溶解し、この油相成分Aを水相成分Bに添加して乳化機で乳化し、この乳化物を攪拌しながら室温まで冷却して、所望する乳液を得た。 (Production Method) The oil phase component A and the water phase component B are dissolved at 70 ° C., the oil phase component A is added to the water phase component B, emulsified with an emulsifier, and the emulsion is stirred to room temperature. Upon cooling, the desired emulsion was obtained.
<実施例23>
本発明品をクリームに応用した。
質量%
A.油相
デシルテトラデカノール 0.2
オリーブ油 10.0
ラノリン 3.0
トリ2−エチルヘキサン酸グリセリル 3.0
パラメトキシケイ皮酸2−エチルヘキシル 2.0
酢酸dl−α−トコフェロール 0.5
パラオキシ安息香酸エチル 0.1
B.水相
プロピレングリコール 5.0
ヒアルロン酸ナトリウム 0.1
エデト酸三ナトリウム 0.1
PEMULEN TR−2 6.0
カルボキシメチルセルロース 0.8
水酸化カリウム 2.5
本発明品 5.5
イオン交換水 残 余<Example 23>
The product of the present invention was applied to a cream.
mass%
A. Oil phase Decyltetradecanol 0.2
Olive oil 10.0
Lanolin 3.0
Glyceryl tri-2-ethylhexanoate 3.0
2-Ethylhexyl paramethoxycinnamate 2.0
Dl-α-tocopherol acetate 0.5
Ethyl paraoxybenzoate 0.1
B. Aqueous phase Propylene glycol 5.0
Sodium hyaluronate 0.1
Edetate trisodium 0.1
PEMULEN TR-2 6.0
Carboxymethylcellulose 0.8
Potassium hydroxide 2.5
Invention product 5.5
Ion exchange water
(製法)油相成分A及び水相成分Bをそれぞれ70℃で溶解し、この油相成分Aを水相成分Bに添加して乳化機で乳化して、この乳化物を攪拌して室温まで冷却して、所望するクリームを得た。 (Manufacturing method) Oil phase component A and aqueous phase component B are each dissolved at 70 ° C., this oil phase component A is added to aqueous phase component B and emulsified with an emulsifier, and this emulsion is stirred to room temperature. Cooled to obtain the desired cream.
<実施例24>
本発明品を乳液に応用した。
質量%
A.油相
流動パラフィン 10.0
ホホバ油 4.0
オレイルアルコール 8.0
2−エチルヘキサン酸セチル 3.0
ビタミンA油 0.1
B.水相
アルブチン 2.0
アスコルビン酸リン酸マグネシウム 1.0
プラセンタエキス 0.5
ヘチマエキス 2.0
PEMULEN TR−1 0.02
CARBOPOL 941 0.15
2−アミノ−2−メチル−1−プロパノール 0.3
エデト酢酸ナトリウム 0.15
パラオキシ安息香酸メチル 0.1
フェノキシエタノール 0.2
本発明品 5.3
イオン交換水 残 余<Example 24>
The product of the present invention was applied to an emulsion.
mass%
A. Oil phase Liquid paraffin 10.0
Jojoba oil 4.0
Oleyl alcohol 8.0
Cetyl 2-ethylhexanoate 3.0
Vitamin A oil 0.1
B. Aqueous phase Arbutin 2.0
Magnesium ascorbate phosphate 1.0
Placenta extract 0.5
Loofah extract 2.0
PEMULEN TR-1 0.02
CARBOPOL 941 0.15
2-Amino-2-methyl-1-propanol 0.3
Sodium edetacetate 0.15
Methyl paraoxybenzoate 0.1
Phenoxyethanol 0.2
Invention product 5.3
Ion exchange water
(製法)上記油相成分A及び水相成分Bをそれぞれ70℃で溶解し、この油相成分Aを水相成分Bに添加して乳化機で乳化し、この乳化物を攪拌しながら室温まで冷却して、所望する乳液を得た。 (Production Method) The oil phase component A and the water phase component B are dissolved at 70 ° C., the oil phase component A is added to the water phase component B, emulsified with an emulsifier, and the emulsion is stirred to room temperature. Upon cooling, the desired emulsion was obtained.
<実施例25:化粧品官能評価テスト>
上記実施例19〜24(クリームまたは乳液)の効果を確認した。評価方法は、実施例18に従った。なお、比較例として、実施例19及び20において、本発明品のみを含まず、その他の含有量は同じものを用いた。
25〜60歳(平均年齢43.0)の男女(各20名)を対象に、それぞれの水溶液0.1mlを左右の手の甲に単回塗布するパネルテストを実施した。
被検者には塗布する被検物の内容は知らせないシングルブラインド試験を実施した。結果を表12に示した。<Example 25: Cosmetic sensory evaluation test>
The effect of the above Examples 19 to 24 (cream or milky lotion) was confirmed. The evaluation method was in accordance with Example 18. As comparative examples, in Examples 19 and 20, only the product of the present invention was not included, and the other contents were the same.
A panel test was performed on males and females (20 people each) between 25 and 60 years old (average age 43.0) by applying 0.1 ml of each aqueous solution to the back of each hand.
A single blind test was conducted in which the subject was not informed of the contents of the test object to be applied. The results are shown in Table 12.
このように、本発明品を含有する化粧品によれば、さっぱりした使用感を保ちつつ、優れた皮膚改善効果を有し、さらに従来から乳化剤として汎用されてきた界面活性剤を配合することなしに経時安定性に優れた、化粧料として用いることのできる乳化組成物を提供できた。
このように、チアシードからチアシードの外殻粘性多糖類と、種子本体・内部の組成物である脂質、たんぱく質、灰分、食物繊維多糖類とを分離して提供することが可能となり、食品、化粧品素材としての応用範囲を広げられた。Thus, according to the cosmetics containing the product of the present invention, while maintaining a refreshing feeling of use, it has an excellent skin improvement effect, and further, without blending a surfactant that has been widely used as an emulsifier conventionally. The emulsion composition which was excellent in stability with time and can be used as a cosmetic can be provided.
In this way, it is possible to separate and provide the chia seed outer viscous polysaccharide from the chia seed and the seed body / internal composition lipid, protein, ash, and dietary fiber polysaccharide. As an application range was expanded.
Claims (14)
淡白色から白色であり、660nmの波長で測定したABS値が0.1%水溶液で0.008以下で透明、1%水溶液で0.200〜0.500であって、前記多糖類の分子量が、5×103〜1×107であり、多糖類異臭がないものである粉末状組成物。
Add 10-20 times the amount of water to the chia seeds, swell the chia shell polysaccharides around the seeds, apply physical force, and remove the seeds of the chia shell polysaccharides obtained by removing the seeds. A powder composition comprising a main component, wherein the physical force is a centrifugal treatment after treatment with a stirrer, and the treatment with the stirrer is performed at a rotational speed of 3000 rpm or 4500 rpm, with a stirring blade And the clearance between the outer wall and the outer wall is obtained by stirring under conditions of 10 mm, 50 mm or 100 mm,
Light white to white, ABS value measured at a wavelength of 660 nm is 0.18 aqueous solution, 0.008 or less, transparent, 1% aqueous solution is 0.200-0.500, and the molecular weight of the polysaccharide is 5 × 10 3 -1 × A powdered composition which is 10 7 and has no odor of polysaccharides.
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